Canonical Allele Identifier: CA802056785
Gene:

Linked Data

ClinVar Variation Id: 646438
ClinVar RCV Id: RCV002534650
dbSNP Id: rs1156546602
MyVariant Identifiers: chr5:g.112043034_112043035insT (hg19) chr5:g.112707337_112707338insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707338dup , CM000667.2:g.112707338dup GRCh38
NC_000005.9:g.112043035dup , CM000667.1:g.112043035dup GRCh37
NC_000005.8:g.112070934dup NCBI36
NG_008481.4:g.19818dup , LRG_130:g.19818dup
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